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Novartis AG (NVS)

NYSE - Nasdaq Real-time price. Currency in USD
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115.97+0.27 (+0.23%)
At close: 04:00PM EDT
116.60 +0.63 (+0.54%)
After hours: 07:16PM EDT
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Trade prices are not sourced from all markets
Previous close115.70
Open116.30
Bid0.00 x 900
Ask0.00 x 800
Day's range115.60 - 116.63
52-week range92.19 - 120.92
Volume771,304
Avg. volume1,235,836
Market cap234.791B
Beta (5Y monthly)0.50
PE ratio (TTM)23.72
EPS (TTM)4.89
Earnings date29 Oct 2024
Forward dividend & yield3.78 (3.26%)
Ex-dividend date07 Mar 2024
1y target est117.31
  • Yahoo Finance Video

    Weight loss drug pricing under fire with pills on the horizon

    Senior health reporter Anjalee Khemlani joins Brad Smith and Madison Mills on Catalysts to take a look at pharmaceutical stocks like Novartis (NVS) and Novo Nordisk (NVO) as weight loss drug makers are set to meet with lawmakers like Senator Bernie Sanders to discuss pricing. Khemlani provides insight into the weight loss drug market and pricing in the US compared to other countries around the world. She explains that Pfizer (PFE), Eli Lilly (LLY), and Novo are among the candidates who could offer weight loss drugs in pill form rather than through injection, which could transform the market. For more expert insight and the latest market action, click here to watch this full episode of Catalysts. This post was written by Naomi Buchanan.

  • Zacks

    Novartis Wins FDA Approval of Kisqali for Early Breast Cancer

    The FDA approves NVS' Kisqali to reduce the risk of disease recurrence in patients with HR+/HER2- early breast cancer.

  • GlobeNewswire

    FDA approves Novartis Kisqali® to reduce risk of recurrence in people with HR+/HER2- early breast cancer

    Ad hoc announcement pursuant to Art. 53 LR Broad indication in HR+/HER2- stage II and III early breast cancer (EBC) at high risk of recurrence approximately doubles population eligible for CDK4/6 inhibitor adjuvant therapy1,2Kisqali® (ribociclib) significantly reduced the risk of recurrence by 25% vs. endocrine therapy (ET) alone; consistent benefit and a well-tolerated safety profile seen across all subgroups in pivotal Phase III NATALEE trial, including patients with node-negative disease3-6La